Alung Technologies Inc

FDA Filings

This page includes the latest FDA filings for Alung Technologies Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009763347
FEI Number3009763347
NameALUNG TECHNOLOGIES INC
Owner & OperatorALung Technologies INC
Contact Address2500 Jane Street Suite 1
Pittsburgh PA 15208 US
Official Correspondent
  • Frank J Falcione
  • x-412-6973370-201
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2500 Jane St Suite 1
Pittsburgh, PA 15203 US
Establishment TypeManufacture Device in the United States for Export Only



FDA Filings

Device
Company
DeviceDate
Alung Technologies, Inc.
Hemolung® Cartridge Spare Parts Kit 2023-03-01
Alung Technologies, Inc.
Hemolung® Catheter Spare Parts Kit 2023-03-01
Alung Technologies, Inc.
Hemolung® 15.5 Fr Jugular Catheter Kit 2023-03-01
Alung Technologies, Inc.
Hemolung® 15.5 Fr Femoral Catheter Kit 2023-03-01
Alung Technologies, Inc.
Hemolung® Cartridge with Blood Tubing 2023-03-01
Alung Technologies, Inc.
Hemolung® Rinse Back Kit 2023-03-01
Alung Technologies, Inc.
Hemolung® Accessories Kit 2023-03-01
Alung Technologies, Inc.
Hemolung® Cartridge Kit 2023-03-01
Alung Technologies, Inc.
Hemolung® CR4 Controller 2023-03-01
ALUNG TECHNOLOGIES INC
Hemolung Respiratory Assist System2012-08-01

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